A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv117n209



Internal ID22826192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205647100..205648139hg38UCSC Ensembl
chr1:205616228..205617267hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381040
hg191040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5887348, nsv5877350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv117n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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